GOODSENSE DIAPER RASH- zinc oxide paste

Goodsense Diaper Rash by

Drug Labeling and Warnings

Goodsense Diaper Rash by is a Otc medication manufactured, distributed, or labeled by Geiss, Destin & Dunn, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                                                   Purpose

Zinc oxide 40%......................................................... Skin protectant

PURPOSE

Uses

• helps treat and prevent diaper rash
• protects chafed skin due to diaper rash and helps seal out wetness

WARNINGS

Warnings

For external use only

WHEN USING

When using this product

• do not get into eyes

STOP USE

Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Directions

• change wet and soiled diapers promptly
• cleanse the diaper area
• allow to dry
• apply paste liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged

STORAGE AND HANDLING

Other information

• store at 20° to 25°C (68° to 77°F)
• Lot No. & Exp. Date: see box or see crimp of tube

INACTIVE INGREDIENT

Inactive ingredients butylhydroxyanisole, lavender oil, liquid paraffin, methylparaben, petrolatum, polysorbate 60, purified lanolin, sorbitan monostearate, squalane, talc, tocopherol, acetate, water

DOSAGE & ADMINISTRATION

Distributed by:

Geiss, Destin & Dunn, Inc.

Peachtree City, GA 30269

www.valuelabels.com

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOODSENSE DIAPER RASH 
zinc oxide paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50804-779
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	400 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
LAVENDER OIL (UNII: ZBP1YXW0H8)
PARAFFIN (UNII: I9O0E3H2ZE)
METHYLPARABEN (UNII: A2I8C7HI9T)
PETROLATUM (UNII: 4T6H12BN9U)
POLYSORBATE 60 (UNII: CAL22UVI4M)
LANOLIN (UNII: 7EV65EAW6H)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
SQUALANE (UNII: GW89575KF9)
TALC (UNII: 7SEV7J4R1U)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50804-779-04	1 in 1 BOX
1		113 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/05/2016

Labeler - Geiss, Destin & Dunn, Inc. (076059836)